Control of the Crystallization Process and Structure Dimensionality of Mg鈥揃enzene鈥?,3,5-Tricarboxylates by Tuning Solvent Composition
详细信息    查看全文
文摘
Four new magnesium 1,3,5-benzenetricarboxylate metal鈥搊rganic framework materials (NICS-n; n = 3鈥?) were synthesized solvothermally in the presence of solvents with different EtOH/H2O ratios. We showed that the crystallization process of the Mg鈥?,3,5-benzentricarboxylate system strongly depends on the solvent composition, and that dimensionality of their structures can be tuned by changing the EtOH/water ratios in the reaction mixture. The presence of only water as a solvent yields the zero-dimensional molecular structure of Mg(H2BTC)2(H2O)4 (NICS-3). One-dimensional (1D) chainlike Mg3(BTC)2(H2O)12 (NICS-4) and two-dimensional (2D) layered Mg2(BTC)(OH)(H2O)4路2H2O (NICS-5) structures were crystallized from EtOH/H2O mixtures with molar ratios of 0.3 and 0.4鈥?.7, respectively. The crystallization in pure ethanol yields Mg3(BTC)2 material (NICS-6) with three-dimensional structure. Nuclear magnetic resonance investigations indicated that bulkier clusters of Mg species are formed in ethanol-rich solutions, even in the absence of the BTC ligand, and that the starting precursors formed with the reaction of Mg species and the BTC ligand at room temperature does not represent the final structures obtained by solvothermal reactions. NICS-4 and NICS-5 are formed from similar starting precursors but slightly different EtOH/H2O ratios causing the crystallization to go in two different directions. Systematic investigation of phase formation using different EtOH/H2O ratios, times, and temperatures of the synthesis along with the computational DFT studies confirmed that the 2D NICS-5 structure represents a thermodynamically more stable phase than 1D chainlike NICS-4. We showed that solvothermal reaction between Mg-precursors and the BTC ligand in EtOH/water mixture represents a complex and sensitive thermodynamic process.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700